| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:53373414-53373512 | Rare:27 | ||||
| chr16:54080673-54080719 | Rare:6 | ||||
| chr16:56617377-56617552 | Common:3; Rare:36 | ||||
| chr16:57039215-57039364 | Rare:19 | ||||
| chr16:57299882-57300011 | Common:6; Rare:94 | ||||
| chr16:65123328-65123350 | Rare:4 | ||||
| chr16:66133964-66134286 | Common:1; Rare:62 | ||||
| chr16:66695975-66696073 | Rare:26 | ||||
| chr16:67390276-67390633 | Common:1; Rare:110 | ||||
| chr16:67483140-67483202 | Common:1; Rare:16 | ||||
| chr16:67563460-67563794 | Rare:107 | ||||
| chr16:67945955-67946324 | Rare:118 | ||||
| chr16:67998576-67998643 | Common:1; Rare:16 | ||||
| chr16:69323922-69324424 | Common:4; Rare:139 | ||||
| chr16:69691529-69691916 | Common:1; Rare:66; Clinvar (benign):2 |